Senior Clinical Research Associate - Psychiatry - East Coast

Worldwide Clinical Trials • Research Triangle Park, NC

2d • Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that pushes boundaries and innovates to find cures for persistent diseases. We are a global team of over 3,500+ experts dedicated to changing the way the world experiences CROs. Our mission is to work with passion and purpose every day to improve lives. We believe everyone plays an important role in making a world of difference for patients and their caregivers. We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity, and we are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Within Clinical Operations, your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will work alongside brilliant minds across diverse therapeutic areas. Collaboration with top-tier colleagues is ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are committed to advancing science and making a difference in the lives of patients around the world. We offer an unparalleled experience where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial.

Requirements

• 5+ years of experience as a Clinical Research Associate
• 4-year university degree OR Nursing Degree
• Experience in Psychiatry is required
• Candidates must reside in the East Coast United States
• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to detail
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS, and EDC Systems

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
• Conduct study initiation visits (SIVs)
• While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

Benefits

• We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior